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- source_evidence_literature type ECO_0000212 NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.
- NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_assertion description "[If no causative ENG or ACVRL1 mutation is found, proband samples are referred for sequence analysis of MADH4 (associated with a combined syndrome of juvenile polyposis and HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.
- NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_assertion evidence source_evidence_literature NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.
- NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_assertion SIO_000772 16690726 NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.
- NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_assertion wasDerivedFrom befree-20150227 NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.
- NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_assertion wasGeneratedBy ECO_0000203 NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP374832.RAkpCyPrlE5lCWu-j_A6UhBgNAice9OTPCX9cMBgOl-KY130_provenance.